Clinical Trial Manager CTM Corcept Therapeutics IncClinical Trial Manager CTMRedwood City, CA$156,600–$184,300 / yearWith advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Manages, either directly or through supervised delegation, other study-wide activities such as external vendors, sample handling, drug re-supply, investigator payments, overall data quality, and overall central records quality.
Clinical Trial Assistant Sagimet Biosciences IncClinical Trial AssistantFoster City, CAThe CTA will play a hands-on role in trial start-up, maintenance, and close-out activities, partnering closely with Clinical Trial Managers (CTMs),, vendors, and cross-functional internal stakeholders. The Clinical Trial Assistant (CTA) provides operational and administrative support to the Clinical Operations team in the execution of Sagimet's clinical trials.
Associate Director, Research Strategic Planning And Operation-Project Management Vir Biotechnology, Inc.Associate Director, Research Strategic Planning And Operation-Project ManagementSan Francisco, CA$162,500–$227,500 / yearThe successful candidate will be a highly collaborative, proactive, and independent leader with strong scientific acumen, excellent communication skills, and demonstrated experience managing complex cross-functional programs in biotechnology or pharmaceutical research environments. Ability balance tactical execution and strategic leadership, from managing project plans, timelines, and meeting logistics to driving cross-functional alignment and facilitating strategic decision-making across all stages of development and levels of leadership.
Research Administration Manager UCSF Medical CenterResearch Administration ManagerSan Francisco, CA10% Leads the organization, planning, establishment and monitoring of fiscal budget control of contracts and grants administration, submissions, budgets, support documents, gifts, endowments and privately funded projects for faculty research programs and departmental operating budgets; Initiates and maintains ongoing, timely and effective communication with all relevant parties throughout the entire post-award process (e.g. This position will provide analytical and financial expertise and leadership for a team of Research Financial Analysts who support contracts and grant administration including post-award fund management activities associated with invoicing, forecasting, planning and managing of research portfolios, and closeout for federal, state, local, private sponsors, and clinical trials for the Hematology and Oncology Division.
NewLife Sciences Research Associate – Regenerative Medicine PAVIRLife Sciences Research Associate – Regenerative MedicinePalo Alto, CAFull timeStrong scientific writing skills and demonstrated capacity to drive first author publications;Knowledge of safe handling/storage of biohazardous chemicals & bloodborne pathogens;Solid training in general lab skills such as micro-pipetting, PCR analysis, cell culture, immunofluorescence staining, and biomaterials characterization;Solid training in analytical skills, including routine calculations of dilution factors and solution concentrations as well as using Excel and other programs for data calculation and analysis or biostatistical analysis;Knowledge of research procedures and protocols gained through education or experience;Experience in a variety of research techniques/methods and follow-up data collection;Knowledge of laboratory safety rules and procedures;Excellent communication skills (written and verbal), including public speaking skills;Ability to work independently and proactively;Ability to work within a team context and collaborate with other lab personnel. on the design and execution of laboratory experiments; Serve as the main contact for experiments;Develop and validate experimental protocols;Analyze data from experiments; Prepare charts for presentations and publication;Write papers on projects for publication;Perform general lab organization; Guide and train lab technicians or other lab members;Other research activities as assigned.
Senior Director, Clinical Data Management Revolution Medicines, Inc.Senior Director, Clinical Data ManagementRedwood City, CA$244,000–$305,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. The Opportunity: The Senior Director of Clinical Data Management provides high-level leadership for data management functions within clinical research, focusing on strategic development, operational execution, and regulatory compliance to ensure data integrity for clinical trials.
NewLife Sciences Research Associate II - Regenerative Medicine PAVIRLife Sciences Research Associate II - Regenerative MedicinePalo Alto, CAFull timeQUALIFICATIONS Required: PhDAt least three years of prior research experience in biology, bioengineering, cell biology, molecular biology or a related discipline (can include during studies);Advanced knowledge of scientific research methodology;Ability to troubleshoot an experiment as necessary;Exquisite record keeping and experimental documentation capabilities;Excellent organizational skills;Strong scientific writing skills and demonstrated capacity to drive first author publications;Knowledge of safe handling/storage of biohazardous chemicals & bloodborne pathogens;Solid training in general lab skills such as micro-pipetting, PCR analysis, genomic and plasmid DNA preparation, protein measurements, and tissue homogenization;Solid training in biomaterials fabrication and characterizationSolid training in analytical skills, including routine calculations of dilution factors and solution concentrations as well as using Excel and other programs for data calculation and analysis;Knowledge of research procedures and protocols gained through education or experience;Experience in a variety of research techniques/methods and follow-up data collection;Knowledge of laboratory safety rules and procedures;Excellent communication skills (written and verbal), including public speaking skills;Ability to work independently and proactively;Ability to work within a team context and collaborate with other lab personnel. on the design and execution of laboratory experiments; Serve as the main contact for experiments;Develop and validate experimental protocols;Analyze data from experiments; Prepare charts for presentations and publication;Write papers on projects for publication;Perform general lab organization; Guide and train lab technicians.
Clinical Contracts Associate Integrated Resources, IncClinical Contracts AssociateFoster City, CaliforniaContractorContractual background - doesn't necessarily need to be in clinical research, but able to understand clinical contracts is importantPreviously seen people with experience in business administration, clinical research, business analysts that reviewed contractors, legal backgroundsNot looking for people with accounts payable backgroundPreviously worked in CRO or clinical sitesAdditional InformationFeel free to forward my email to your friends/colleagues who might be available. IT Life Sciences Allied Healthcare CRODIRECT # - (732)-844-8715Gold Seal JCAHO Certified for Health Care Staffing"INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)
Senior Research Associate KariusSenior Research AssociateRedwood City, CABy unlocking the information present in microbial cell-free DNA, we're helping doctors quickly solve their most challenging cases, providing industry partners with access to the microbial landscape to accelerate biomarker discovery and clinical trials, discover novel microbes, to ultimately reduce patient suffering worldwide. The company’s platform is already delivering unprecedented insights into the microbial landscape, providing clinicians with a comprehensive test capable of identifying more than a thousand pathogens directly from blood, and helping industry accelerate the development of therapeutic solutions.
Clinical Trial Associate Ardelyx IncClinical Trial AssociateNewark, CA$86,000–$105,000 / yearPosition Summary: The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of assigned clinical trials, ensuring operational excellence, compliance with ICH-GCP and applicable regulatory requirements, and adherence to study timelines. The CTA contributes across all phases of the clinical trial lifecycle, from study start-up through close-out, and is responsible for the timely execution of study activities and deliverables in alignment with clinical development objectives and corporate goals.
Technical Research Assistant Cellular Neuropsychiatry Lab Stem Mass General BrighamTechnical Research Assistant Cellular Neuropsychiatry Lab StemBelmont, CaliforniaThe Laboratory of Cellular Neuropsychiatry in the Program for Neuropsychiatric Research at McLean Hospital investigates disease specific differences in two major cellular pathways: myelination and bioenergetics using induced pluripotent stem cells (iPSC) as a model system. Working under the general supervision and following established policies and procedures, conducts a variety of specialized experimental procedures in human iPS cell culture and differentiation, human fibroblast culture, fluorescence microscopy, FACS analysis, cell biology assays and molecular biology techniques.
Founding Engineer, Applied Research Backbone SystemsFounding Engineer, Applied ResearchSan Francisco, CaliforniaBackbone’s core systems, based on post-trained open-weights models and systems of closed-weights models, read charts, claims, denials, appeals, clinical criteria, payer policies, and quality metrics, then make accurate, defensible decisions in production. Today, U.S. healthcare wastes more than $350B yearly on administrative work that has nothing to do with patient care: prior authorizations, denials, appeals, and the staff hired on both sides of the aisle to adjudicate and determine payment for services rendered.
Research Data Scientist StratAcuity Staffing Partners IncResearch Data ScientistPleasanton, CA$75–$83 / hourIn terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. The work is project-based, research-driven, and highly collaborative, requiring a high level of technical breadth and autonomy to help researchers translate scientific questions into operational workflows.
Vice President (Vp) / Senior VP, Clinical Development Lycia TherapeuticsVice President (Vp) / Senior VP, Clinical DevelopmentSouth San Francisco, CA$360,000–$420,000 / yearCollaboration with the Lycia Executive Committee members, early development / translational medicine leader, internal cross functional team members, as well as partner with contract research organizations (CROs), investigators and study site staff, and external consultants to advance multiple drug candidates, including into mid- and late-stage development. Provide medical support related to the development of medical and/or relevant scientific sections of clinical study and/or regulatory documents (e.g., study protocol, investigators brochure, informed consent forms, clinical study reports, statistical analysis plans, safety updates / annual safety reports, responses to Health Authorities and/or Ethics Committees / Institutional Review Committees).
Sr. Research Associate/Associate Scientist, Nonclinical Development Adicet BioSr. Research Associate/Associate Scientist, Nonclinical DevelopmentRedwood City, CaliforniaAdicet is located in a state-of-the-art facility and works to create an incredible office experience with an onsite gym and various other fitness options, onsite parking with electric vehicle charging stations and free shuttle (Caltrain), company-subsidized lunches (delivered onsite daily) and fully stocked breakrooms. Coordinate and execute in vivo and ex vivo nonclinical studies to evaluate Adicet’s immune-cell and gene-therapy platforms, including efficacy, pharmacokinetic/pharmacodynamic, and safety assessments in relevant murine oncology and immunology models.
Research Scientist Galvanize Therapeutics IncResearch ScientistRedwood City, CA$115,000–$130,000 / yearThey are focused on the translational and clinical science analysis of advanced biological and clinical outcomes phenomena, particularly in relation to cellular, tissue, and immunological responses to pulsed electric fields (PEFs). They may support external research projects, including consulting on and performing biological analyses, as well as travel to assist with delivery of modified Aliya protocols at external research facilities under Research Grant Agreements.
Clinical data manager Integrated Resources, IncClinical data managerFoster City, CaliforniaContractorWorks collaboratively with Biomarker Clinical Operations team members, Biomarker Scientists, Biomarker Statistical Programming group, Biomarker Biostatistics group, Biomarker Clinical Programming group, Bio banking and Sample Management group, and lead study clinical data associate and cross-functional study team members to meet project deliverables and timelines for biomarker data acquisition, quality checking and reporting. QualificationsLead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experienceUnderstanding of clinical data management processesProject management experience of clinical trialsCommunication with cross-functional study team members
Executive Director, Clinical Science, Oncology, Hematology, Oncology Assets and Early Development Merck & Co IncExecutive Director, Clinical Science, Oncology, Hematology, Oncology Assets and Early DevelopmentSouth San Francisco, CA$255,800–$402,700 / yearRequired Skills: Advanced Analytics, Artificial Intelligence (AI), Clinical Development, Clinical Sciences, Cross-Functional Leadership, Executive Leadership, Global Clinical Studies, Innovation, Matrix Leadership, Oncology, Oncology Drug Development, Regulatory Submissions, Strategic Leadership, Talent Development. The Executive Director, Clinical Science is a senior leader within Oncology Clinical Development responsible for providing strategic, scientific, operational, and people leadership across a portfolio of oncology programs spanning multiple therapeutic areas (Hematology, Oncology Assets and Early Development) and stages of development.
Sr. Clinical Trial Management Associate Integrated Resources, IncSr. Clinical Trial Management AssociateFoster City, CaliforniaContractorInterfaces with individuals in other functional areas to address routine study issuesAbility to develop tools and processes that increase measured efficiencies of the projectMay be asked to assist in the training of CTMAs and CPAsAssists in CRO or vendor selectionCoordinates CROs or vendorsAssists in the setting and updating of study timelinesMust be able to participate in departmental or interdepartmental strategic initiatives under general supervisionAssists in the review of routine data and preparation of safety, interim, and final study reports, and resolution of data discrepanciesMay conduct site evaluation, initiation, co-monitoring, and closeout visits in addition to routine monitoring visits, as requiredAssures site compliance with the protocol and regulatory requirementsDrafts and coordinates review of protocols, informed consents, case report forms and monitoring plansExcellent verbal, written, interpersonal and presentation skills are requiredKnowledge of FDA and or EMA Regulations, ICH Guidelines, and GCP governing the conduct of clinical studiesWorking knowledge and experience with Word, PowerPoint and ExcelQualificationsMinimum Education And ExperienceAt least 3+ years of experience and a BS or BA in a relevant scientific disciplineAdditional InformationKind Regards,Sabanaaz ShaikhClinical RecruiterIntegrated Resources, Inc. Clinical Trials Management AssociateDuration: 6 MonthsLocation: Foster City, CA, United StatesJob Responsibilities And SkillsMust meet all requirements for CTMA position and have demonstrated proficiency in all relevant areasMust be able to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and proceduresParticipates or effectively runs meetings and conference calls with CROs, vendors, and multi-functional teamsMust be able to anticipate obstacles and proactively develop solutions to achieve project goalsMust have a general understanding of functional issues and routine project goals from an organizational perspectiveMay participate in abstract presentations, oral presentations and manuscript development.
Senior Research Associate Cytokinetics, IncorporatedSenior Research AssociateSouth San Francisco, CA$108,000–$126,000 / yearCytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction. Design and perform high-content imaging (HCI) assays using skeletal and/or cardiac muscle cell models, including image acquisition, analysis, and interpretation of complex datasets.